Relevant bibliographies by topics / Pharmaceutical chemistry – Research – Analysis

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Pharmaceutical chemistry – Research – Analysis'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Pharmaceutical chemistry – Research – Analysis"

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Berendt, Robert T., Diana M. Sperger, Eric J. Munson, and Paul K. Isbester. "Solid-state NMR spectroscopy in pharmaceutical research and analysis." TrAC Trends in Analytical Chemistry 25, no. 10 (November 2006): 977–84. http://dx.doi.org/10.1016/j.trac.2006.07.006.

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Jansson, Sven Olof, and J�rgen Vessman. "Trends in product analysis for research in the pharmaceutical industry." Mikrochimica Acta 104, no. 1-6 (January 1991): 103–12. http://dx.doi.org/10.1007/bf01245501.

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Niculet, Elena, Gina Vica Neculia, Alin Laurentiu Tatu, and Olimpia Dumitriu Buzia. "Curcumin- Extraction, Physical and Chemical Analysis, Formulas and Control. Basic Methods for Further Research." Materiale Plastice 55, no. 4 (December 30, 2018): 672–75. http://dx.doi.org/10.37358/mp.18.4.5110.

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Turmeric, with its active component curcumin has been regarded lately as an important potential therapeutic agent due to its properties and many uses. Further research needs to be done both on animals and humans in order for it to be used at a large scale. As curcumin gets absorbed better through topical and not oral administration, curcumin-based pharmaceuticals with skin passage must be devised. In order for this to be done, the need for a standardized, verified and simple extraction method and one for ointment preparation with stability in time rises. We propose in this study a method for curcumin extraction, one that ensures an adequate stability in time and a method for pharmaceutical control.
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Bruni, Renato, Davide Barreca, Michele Protti, Virginia Brighenti, Laura Righetti, Lisa Anceschi, Laura Mercolini, Stefania Benvenuti, Giuseppe Gattuso, and Federica Pellati. "Botanical Sources, Chemistry, Analysis, and Biological Activity of Furanocoumarins of Pharmaceutical Interest." Molecules 24, no. 11 (June 8, 2019): 2163. http://dx.doi.org/10.3390/molecules24112163.

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The aim of this work is to provide a critical review of plant furanocoumarins from different points of view, including their chemistry and biosynthetic pathways to their extraction, analysis, and synthesis, to the main biological activities found for these active compounds, in order to highlight their potential within pharmaceutical science. The limits and the possible improvements needed for research involving these molecules are also highlighted and discussed.
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Sutariya, Vijaykumar, Anastasia Groshev, Prabodh Sadana, Deepak Bhatia, and Yashwant Pathak. "Artificial Neural Network in Drug Delivery and Pharmaceutical Research." Open Bioinformatics Journal 7, no. 1 (December 13, 2013): 49–62. http://dx.doi.org/10.2174/1875036201307010049.

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Artificial neural networks (ANNs) technology models the pattern recognition capabilities of the neural networks of the brain. Similarly to a single neuron in the brain, artificial neuron unit receives inputs from many external sources, processes them, and makes decisions. Interestingly, ANN simulates the biological nervous system and draws on analogues of adaptive biological neurons. ANNs do not require rigidly structured experimental designs and can map functions using historical or incomplete data, which makes them a powerful tool for simulation of various non-linear systems.ANNs have many applications in various fields, including engineering, psychology, medicinal chemistry and pharmaceutical research. Because of their capacity for making predictions, pattern recognition, and modeling, ANNs have been very useful in many aspects of pharmaceutical research including modeling of the brain neural network, analytical data analysis, drug modeling, protein structure and function, dosage optimization and manufacturing, pharmacokinetics and pharmacodynamics modeling, and in vitro in vivo correlations. This review discusses the applications of ANNs in drug delivery and pharmacological research.
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Pedro, Sónia N., Carmen S. R. Freire, Armando J. D. Silvestre, and Mara G. Freire. "The Role of Ionic Liquids in the Pharmaceutical Field: An Overview of Relevant Applications." International Journal of Molecular Sciences 21, no. 21 (November 5, 2020): 8298. http://dx.doi.org/10.3390/ijms21218298.

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Solubility, bioavailability, permeation, polymorphism, and stability concerns associated to solid-state pharmaceuticals demand for effective solutions. To overcome some of these drawbacks, ionic liquids (ILs) have been investigated as solvents, reagents, and anti-solvents in the synthesis and crystallization of active pharmaceutical ingredients (APIs), as solvents, co-solvents and emulsifiers in drug formulations, as pharmaceuticals (API-ILs) aiming liquid therapeutics, and in the development and/or improvement of drug-delivery-based systems. The present review focuses on the use of ILs in the pharmaceutical field, covering their multiple applications from pharmaceutical synthesis to drug delivery. The most relevant research conducted up to date is presented and discussed, together with a critical analysis of the most significant IL-based strategies in order to improve the performance of therapeutics and drug delivery systems.
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Rogers, Michael J., Anshuman Gupta, and Costas D. Maranas. "Real Options Based Analysis of Optimal Pharmaceutical Research and Development Portfolios." Industrial & Engineering Chemistry Research 41, no. 25 (December 2002): 6607–20. http://dx.doi.org/10.1021/ie020385p.

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Starek, Małgorzata, and Monika Dąbrowska. "Chromatographic techniques in analysis of cyclooxygenase-2 inhibitors in drugs and biological samples." Open Chemistry 10, no. 3 (June 1, 2012): 711–30. http://dx.doi.org/10.2478/s11532-012-0029-y.

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AbstractNon-steroidal anti-inflammatory drugs, as a therapeutic class, are among the most often used active pharmaceutical ingredients in heath care in the world. They are mostly available without prescription and often used for treatment of fever and pain. An extensive research of the literature published in analytical and pharmaceutical chemistry journals has been conducted and the chromatographic methods which were used for the purity, stability and pharmacokinetic studies of the cyclooxygenase-2 inhibitors, in formulations and biological materials have been reviewed. The methodology for the analysis of selected drugs is very well documented and many examples are available in the literature. The common use of chromatographic techniques with various detection attachments provide possibility for monitoring of drugs in therapy.
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Custers, Deborah, Patricia Courselle, Sandra Apers, and Eric Deconinck. "Chemometrical analysis of fingerprints for the detection of counterfeit and falsified medicines." Reviews in Analytical Chemistry 35, no. 4 (December 1, 2016): 145–68. http://dx.doi.org/10.1515/revac-2016-0013.

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AbstractCounterfeit medicines pose a major threat to public health worldwide. These pharmaceuticals are mostly manufactured without respecting Good Manufacturing Practices. Moreover, they are not subjected to any form of quality control, and therefore their safety, efficacy, and quality cannot be guaranteed. Extensive research on counterfeit medicines has already been performed and published in literature. This review aims at providing an updated overview of the use of fingerprints and subsequent multivariate (chemometrical) data analysis in the field of counterfeit medicine detection. Fingerprinting could be a useful tool in the analysis of counterfeit medicines because it generates a holistic view of a sample, rather than focusing on specific and predefined characteristics, such as identification and quantification of present active pharmaceutical ingredients. This review first provides an introduction into the counterfeiting problem. Next, the concept of fingerprinting and the basic principles of chemometrics are explained, followed by a description of the successful application of fingerprints in the field of Pharmacognosy. The last part of this review provides an overview describing the use of fingerprints in counterfeit medicine research.
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Pinto, Prakash, Iqbal Thonse Hawaldar, Guruprasad Kemminje, Babitha Rohit, Cristi Marcel Spulbar, Felicia Ramona Birau, and Cristian Valeriu Stanciu. "The Impact of Risk Anomalies on the Pharmaceutical Sector of the Indian Stock Market. A comparative analysis between pharmaceutical, FMCG and IT companies." Revista de Chimie 71, no. 2 (March 3, 2020): 58–63. http://dx.doi.org/10.37358/rc.20.2.7892.

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The main purpose of this research article is to provide a comparative framework on various implications of risk anomalies on Indian stock market based on an empirical study for the following sectors: Pharmaceutical, Fast-Moving Consumer Goods (FMCG) and IT. Risk anomaly is a notable anomaly because it is continual and all-inclusive. This research study aims to examine the existence of risk anomaly in the National Stock Exchange, India, and in particular providing a comparative analysis on the behavior of the pharmaceutical sector in India.
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Dissertations / Theses on the topic "Pharmaceutical chemistry – Research – Analysis"

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Mandimika, Nyaradzo. "Evaluation of the pharmaceutical availability of erythromycin from topical formulations." Thesis, Rhodes University, 2008. http://eprints.ru.ac.za/1176/.

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Wang, Jialu. "Facile Methods for the Analysis of Lysophosphatidic Acids in Human Plasma." PDXScholar, 2015. https://pdxscholar.library.pdx.edu/open_access_etds/2235.

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Lysophosphatidic acid (LPA) influences many physiological processes, such as brain and vascular development. It is associated with several diseases including ovarian cancer, breast cancer, prostate cancer, colorectal cancer, hepatocellular carcinoma, multiple myeloma atherosclerotic diseases, cardiovascular diseases, pulmonary inflammatory diseases and renal diseases. LPA plasma and serum levels have been reported to be important values in diagnosing ovarian cancer and other diseases. However, the extraction and quantification of LPA in plasma are very challenging because of the low physiological concentration and similar structures of LPA to other phospholipids. Many previous studies have not described the separation of LPA from other phospholipids, which may make analyses more challenging than necessary. We developed an SPE extraction method for plasma LPA that can extract LPA at high purity. We also developed an HPLC post-column fluorescence detection method that allows the efficient quantification of LPA. These methods were used in a clinical study for ovarian cancer diagnosis to help validate LPA as a biomarker of ovarian cancer. Moreover, molecular imprinted polymers (MIPs) were designed and synthesized as material for the improved extraction of LPA. Compared to the commercially available materials, the MIP developed shows enhanced selectivity for LPA. The extraction was overall relatively more efficient and less labor-intensive.
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Thakur, Shravan Singh. "Introduction to Pharmaceutical Thermal Analysis: A Teaching Tool." Cleveland State University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=csu1316880806.

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Faulkner, W. "Linkage between industrial and academic research : The case of biotechnological research in the pharmaceutical industry." Thesis, University of Sussex, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373169.

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This thesis is a study of research linkage between industry and academia. It concentrates on the industrial side of these interactions and, in particular, the impact of information flows from academia industrial innovation. Specifically, the study explores the proposition that linkage varies - in extent and nature according to the stage of development of the research field involved. A review of the literature suggested that linkage should be particularly strong in a nascent technology, such as that unfolding currently in biotechnology. The field study involved face-to-face interviews with industrial researchers from UK pharmaceutical companies and from new start-up companies. It was designed in order to ascertain the relative strength of linkages in the new biotechnology; to characterize these linkages; and to explore how they might change as the technology develops. It is ~emonstrated that linkage is indeed strong here, involving lntensive 'search' activities and often substantial formal collaboration with academia. The background material collected - concerning the role of linkage in innovation and in corporate strategies for biotechnology confirm that companies are obliged to 'plug in' to academic research precisely because 'of the dynamism and uncertainty which characterizes a new technological field. It is argued that those pharmaceutical companies which are interacting most with academic research are also those which are most likely to succeed commercially with the new techniques. The start-up companies in biotechnology are shown to have extremely close links with both academia and the large established companies active in the field. It is argued that the very presence of such companies is itself symptomatic of the proximity of academic science and industrial technology in this new field. In conclusion, it is suggested that the pattern of linkage found in biotechnology may well ~ertain in other new science-based fields; some policy lmplications are discussed.
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Enlund, Anna Maria. "Capillary electroseparations in pharmaceutical analysis of basic drugs and related substances." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2001. http://w3.ub.uu.se/fulltext/91-554-4908-5.pdf.

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Han, Guoxia. "Design, synthesis, pharmacology, and structural analysis of bioactive melanocortin receptors' ligands by hybrid approaches." Diss., The University of Arizona, 2000. http://hdl.handle.net/10150/284287.

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A number of alpha-melanotropin (α-MSH) analogues have been designed de novo, synthesized and bioassayed at different melanocortin receptors from frog skins, mice and humans. These ligands were designed from two scaffolds, Somatostatin and Deltorphin-II, by two new hybrid approaches, one of which utilizes the modified cyclic structure (H-DPhe-Cys---Cys-Thr-NH₂) of a Somatostatin analogue--Sandostatin®, while the other incorporates the hydrophobic tail of Deltorphin-II (Glu-Val-Val-Gly-NH₂). Some of the ligands designed, H-DPhe-c [XXX-YYY-ZZZ-Arg-Trp-AAA]-Thr-NH₂ [XXX and AAA = Cys, DCys, Pen, DPen; YYY = His, His(1-Me), His(3-Me); ZZZ = Phe and side chain halogen substituted Phe, DPhe, DNal(1') and DNal(2 ')] and c[XXX-YYY-ZZZ-Arg-Trp-Glu]-Val-Val-Gly-NH₂ [XXX = nothing, Gly, β-Ala, γ-Abu, 6-Ahx; YYY = His, His(3-Bom), (S)-cyclopentylglycine (CPG); ZZZ = Phe, DPhe; DNal(2')], show unique selectivity and potency among the receptors tested. In particular, one of the ligands, Delt-38B--c[Gly-CPG-DNal(2')Arg-Trp-Glu]-Val-Val-Gly-NH₂, is a human melanocortin receptor (hMC1R) antagonist (IC₅₀ = 12 nM) the first potent hMC1R antagonist discovered. These results provide strong evidence supporting our hypothesis that ligand scaffolds for different G-protein coupled receptors (GPCRs) can be used to design ligands for other GPCRs. In addition, the structures of some of the ligands have been analyzed by high field solution NMR and their conformation evaluated by modeling with MacroModel. The conformations obtained from these methods help us better understand the structural basis the selectivities and ligand-receptor interactions.
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Currie, Christa Anne. "Capillary and Microchip Electrophoresis Systems for Pharmaceutical Analysis." University of Cincinnati / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1242998601.

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Randall, Elizabeth Claire. "Development and integration of chemical imaging methods for applications in biomedical and pharmaceutical research." Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7602/.

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Imaging of biomolecules in biological substrates by mass spectrometry or spectroscopic imaging techniques plays a major role in biomedical, clinical, and pharmaceutical research. The work presented in this thesis investigates the capabilities of three imaging techniques, liquid extraction surface analysis (LESA) mass spectrometry imaging (MSI), matrix assisted laser desorption ionisation (MALDI) MSI and stimulated Raman scattering (SRS) microscopy. A method for combined LESA and MALDI analysis was developed and results provided high resolution imaging of multiple analyte classes (proteins, lipids and small molecule drugs) in thin tissue sections. SRS microscopy was used for the quantitative imaging of MALDI sampling effects and sample preparation, providing insight into fundamental processes of MALDI MS. Multimodal SRS, LESA and MALDI imaging was executed on a single tissue sample revealing the complementarity between the three approaches. Specific challenges for LESA were further explored, namely quantification, improved spatial resolution and alternative biological substrates. A quantitative LESA method based on the production of mimetic tissue models containing stable isotope-labelled proteins was developed. An alternative platform, the Flow-Probe™, with the potential to achieve higher spatial resolution was assessed. Finally, a LESA method for the direct analysis of proteins from live bacterial colonies was developed.
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Medeiros, Marina dos Santos Garruti de. "Sensory analysis of extemporaneous formulations of cardiovascular drugs prepared with the vehicle âguteâ and administered to pediatric patients." Universidade Federal do CearÃ, 2014. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=12247.

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CoordenaÃÃo de AperfeÃoamento de Pessoal de NÃvel Superior
Many pediatric patients require medications that are not available in age appropriate formulations, especially those with cardiovascular diseases. Furosemide and Captopril generally are produced in solid dosage forms for adults, and need to be fractionated and transformed in suspensions for use in children. The use of a suitable vehicle is critical to the preparation of a homogeneous, stable and palatable extemporaneous formulation that can guarantee the expected effect. In this work was evaluated the acceptability of a vehicle, named Gute, developed by a research group from Universidade Federal do CearÃ, considering that palatability is essential to treatment adherence in children. We analyzed the vehicle in different flavors with respect to the ability to mask the bitter taste of Captopril and Furosemide, the acceptance and preference without actives by healthy children and their parents, and the acceptance of extemporaneous formulations of the mentioned drugs administered to pediatric patients as prescribed. In the laboratory, eight panelists evaluated the masking ability of the vehicle flavored in mint, cherry, strawberry and neutral using a linear scale. ANOVA scores for bitterness intensity for captopril and furosemide showed that the flavored samples had significantly greater capacity of masking the bitter taste than the vehicle without flavor (neutral), however, there was no different between the flavors. 62 children 4-12 years and 21 guardians participated in the evaluation of the vehicle without actives flavored in mint, strawberry and cherry, using a facial-verbal hedonic scale with seven degrees. The three flavors were accepted and equally preferred by children and guardians. In hospitalized patients who received suspensions of Captopril (34) and furosemide (36), the flavors mint, strawberry and neutral acceptance was evaluated through the guardians with the hedonic scale and compared with the observation of the researcher .Suspensions in neutral and strawberry flavors were considered acceptable for both drugs. The correlation between the results from the two methods was moderate for Captopril, and absent Furosemide. The results for the neutral flavor showed that the addition of flavoring agents did not influenced in the acceptance and can be avoided in this case, an advantage in terms of safety for infants and neonates.
Muitos medicamentos necessÃrios a pacientes pediÃtricos nÃo sÃo disponÃveis em formulaÃÃes apropriadas à idade, principalmente aqueles que tratam doenÃas cardiovasculares. Captopril e Furosemida, de modo geral, sÃo produzidos na forma sÃlida em doses para adultos, e necessitam ser fracionados e transformados em suspensÃes para uso em crianÃas. O uso de um veÃculo adequado à crÃtico para o preparo de formulaÃÃes extemporÃneas homogÃneas, palatÃveis e estÃveis, que possam garantir o efeito esperado. Neste trabalho foi avaliada a aceitabilidade de um veÃculo com nome fantasia Gute, desenvolvido por um grupo de pesquisa da Universidade Federal do CearÃ, tendo em vista que a palatabilidade à essencial para a adesÃo ao tratamento em crianÃas. Analisou-se o veÃculo em diferentes sabores em relaÃÃo à capacidade de mascarar o gosto amargo de Captopril e Furosemida, sua aceitaÃÃo e preferÃncia sem ativos por crianÃas sadias e seus responsÃveis, bem como a aceitaÃÃo de formulaÃÃes extemporÃneas dos medicamentos citados, administradas a pacientes pediÃtricos, conforme prescriÃÃo. Em laboratÃrio, oito provadores avaliaram a capacidade de mascaramento do veÃculo flavorizado nos sabores menta, cereja, morango e neutro, utilizando uma escala linear. A anova dos valores de intensidade do sabor amargo, para Captopril e Furosemida, mostrou que a capacidade dos sabores flavorizados de mascarar o sabor amargo foi significativamente maior do que a do veÃculo sem sabor, contudo, os sabores nÃo diferiram entre si. Participaram da avaliaÃÃo do veÃculo sem ativos, nos sabores menta, morango e cereja, 62 crianÃas de 4 a 12 anos e 21 responsÃveis, usando uma escala hedÃnica facial-verbal de sete graus. Os trÃs sabores foram aceitos e igualmente preferidos pelas crianÃas e pelos responsÃveis. Com os pacientes internados que receberam suspensÃes de Captopril (34) e Furosemida (36), nos sabores menta, neutro e morango, a aceitaÃÃo foi avaliada atravÃs dos responsÃveis com uso da escala hedÃnica e comparada com a observaÃÃo da pesquisadora. As suspensÃes nos sabores neutro e morango foram consideradas aceitas para ambos os medicamentos. A correlaÃÃo entre os resultados provenientes dos dois mÃtodos de avaliaÃÃo da aceitaÃÃo foi moderada para Captopril, e para Furosemida, nÃo houve correlaÃÃo. Os resultados relativos ao sabor neutro mostraram que a adiÃÃo de flavorizantes nÃo influenciou na aceitaÃÃo das suspensÃes, podendo ser evitada nesses casos, uma vantagem em termos de seguranÃa para bebÃs e neonatos.
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Mabotha, Tebogo E. "The application of physicochemical methods for the analysis of small and complex pharmaceutical drugs." Master's thesis, University of Cape Town, 2003. http://hdl.handle.net/11427/6327.

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The application of physicochemical methods for the analysis of small and complex pharmaceutical drugs was investigated. The methods were applied to small chiral molecules and further extended to analysis of complex glycoconjugate vaccines.
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Books on the topic "Pharmaceutical chemistry – Research – Analysis"

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Chʻoe, Chong-gil. Ŭiyakpʻum hamnyang sihŏmpŏp ŭi tayangsŏng e taehan yŏnʼgu =: Study on the analysis for simultaneous assay in pharmaceutical products. [Seoul]: Sikpʻum Ŭiyakpʻum Anjŏnchʻŏng, 2007.

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Mager, Peter P. Multivariate chemometrics in QSAR (quantitative structure-activity relationships): A dialogue. Letchworth, Hertfordshire, England: Research Studies Press, 1988.

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Significant pharmaceuticals reported in recent US patents. Amsterdam: Elsevier, 2007.

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Modern methods of pharmaceutical analysis. 2nd ed. Boca Raton, Fla: CRC Press, 1991.

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Stig, Pedersen-Bjergaard, and Rasmussen Knut, eds. Chemical analysis in pharmaceutical sciences. Chichester, West Sussex: John Wiley & Sons Inc., 2012.

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LC/MS applications in drug development. New York: J. Wiley & Sones, 2002.

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Colombo, Giulia P. Medicinal chemistry research progress. New York: Nova Science Publishers, 2008.

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Szepesi, Gabór. HPLC in pharmaceutical analysis. Boca Raton, Fla: CRC Press, 1990.

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HPLC in pharmaceutical analysis. Boca Raton, Fla: CRC Press, 1990.

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Ford, James L. Pharmaceutical thermal analysis: Techniques and applications. Chichester: E. Horwood, 1989.

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Book chapters on the topic "Pharmaceutical chemistry – Research – Analysis"

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Kawakubo, Hiromu. "Process Research with Explosive Reactions." In Pharmaceutical Process Chemistry, 363–80. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633678.ch18.

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Karpf, Martin. "From Milligrams to Tons: The Importance of Synthesis and Process Research in the Development of New Drugs." In Pharmaceutical Process Chemistry, 1–37. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633678.ch1.

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Patil, Sachinkumar, Shitalkumar Patil, Sudha Kharade, and Dipali Kamble. "Pharmaceutical Interactions in Drug Practices." In Handbook of Research on Medicinal Chemistry, 459–596. Toronto ; New Jersey : Apple Academic Press, 2017.: Apple Academic Press, 2017. http://dx.doi.org/10.1201/9781315207414-12.

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Sahu, Ram Kumar, and Amit Roy. "Pharmaceutical Importance of Natural Aphrodisiac Drugs." In Handbook of Research on Medicinal Chemistry, 163–97. Toronto ; New Jersey : Apple Academic Press, 2017.: Apple Academic Press, 2017. http://dx.doi.org/10.1201/9781315207414-5.

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Scriba, Gerhard K. E. "Chiral electromigration techniques in pharmaceutical and biomedical analysis." In Frontiers of Bioanalytical Chemistry, 225–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-36303-0_11.

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Abramov, Yuriy A. "Theoretical Hydrogen-Bonding Analysis for Assessment of Physical Stability of Pharmaceutical Solid Forms." In Computational Pharmaceutical Solid State Chemistry, 37–56. Hoboken, NJ: John Wiley & Sons, Inc, 2016. http://dx.doi.org/10.1002/9781118700686.ch3.

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Ohemeng-Boahen, Godfred, Divine D. Sewu, Caleb Acquah, and Marc A. Dubé. "CHAPTER 7. Protein-based Bioplastics for Food and Pharmaceutical Packaging." In Food Chemistry, Function and Analysis, 173–206. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839163425-00173.

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Müller, Klaus. "Molecular Modelling and Structural Databases in Pharmaceutical Research." In Bioorganic Chemistry in Healthcare and Technology, 39–52. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-1354-0_4.

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Parasar, Parveen, and Vivek Singh. "Islet Transplantation in Type 1 Diabetes: Stem Cell Research and Therapy." In Medicinal Chemistry with Pharmaceutical Product Development, 33–57. Toronto ; New Jersey : Apple Academic Press, 2019. | Series: AAP research notes on chemistry: Apple Academic Press, 2019. http://dx.doi.org/10.1201/9780429487842-2.

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Morand, Kenneth L., and Xueheng Cheng. "Organic Compound Stability in Large, Diverse Pharmaceutical Screening Collections." In Analysis and Purification Methods in Combinatorial Chemistry, 321–50. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471531979.ch13.

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Conference papers on the topic "Pharmaceutical chemistry – Research – Analysis"

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Zhou, Jianbo, Xiaoying Cui, Chao Xu, Ming Zeng, and Wen Chen. "Preliminary Study Application on qParticipatoryq Teaching Mode in Pharmaceutical Organic Chemistry Experiment." In 2016 5th International Conference on Social Science, Education and Humanities Research. Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/ssehr-16.2016.175.

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Pate, Brooks, Channing West, Reilly Sonstrom, Haley Scolati, Kevin Mayer, and Martin Holdren. "CHEMICAL ANALYSIS CHALLENGES IN PHARMACEUTICAL CHEMISTRY AND UNDERGRADUATE PHYSICAL CHEMISTRY LABORATORY PROJECTS USING ROTATIONAL SPECTROSCOPY." In 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.tb06.

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Zhang, Yixin. "Contributions of Novel Nanomaterials to Pharmaceutical Analysis." In ICBRA '19: 2019 6th International Conference on Bioinformatics Research and Applications. New York, NY, USA: ACM, 2019. http://dx.doi.org/10.1145/3383783.3383796.

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Junping, Zhang, Zhang Aihua, and Wei Zheng. "THE COMPARATIVE ANALYSIS OF COMMON TREATMENT FOR VARICOSE VEINS." In World Congress on Medical and Pharmaceutical Research (WCMPR 2017). Volkson Press, 2018. http://dx.doi.org/10.26480/wcmpr.01.2018.22.24.

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A., Manjunath, Ashwini A., Mahalesh Devandrappa, Balaji Biradar, Mohanraj Pattar, and B. R. Kerur. "Qualitative analysis of pharmaceutical drugs by x-ray transmission method: A non-destructive technique." In PROF. DINESH VARSHNEY MEMORIAL NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS: NCPCM 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5098668.

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Vázquez Álvarez, Ana María, and Gabriela Fernández Saavedra. "THE USE OF SIMULATORS IN THE TEACHING OF PHARMACOLOGY. STUDENTS' OPINION OF THE BACHELOR’S DEGREE IN CHEMISTRY PHARMACEUTICAL-BIOLOGIST." In 12th annual International Conference of Education, Research and Innovation. IATED, 2019. http://dx.doi.org/10.21125/iceri.2019.0421.

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Huan, Li. "ANALYSIS ON THE RELATIONSHIP BETWEEN ACUPUNCTURE AND MOXIBUSTION MASSAGE AND HEALTH CARE." In World Congress on Medical and Pharmaceutical Research (WCMPR 2017). Volkson Press, 2018. http://dx.doi.org/10.26480/wcmpr.01.2018.25.26.

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Yunpeng, Li, Lu Hua, Wu Shuang, Xu Dayong, Yue zongjin, and Wang Xinli. "CLINICAL ANALYSIS OF ACUPUNCTURE THERAPY IN THE TREATMENT OF ARTHRITIS WITH TRADITIONAL CHINESE MEDICINE." In World Congress on Medical and Pharmaceutical Research (WCMPR 2017). Volkson Press, 2018. http://dx.doi.org/10.26480/wcmpr.01.2018.14.16.

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Yunpeng, Li, Lu Hua, Wu Shuang, Xu Dayong, Yue zongjin, and Wang Xinli. "CLINICAL ANALYSIS OF ACUPUNCTURE THERAPY IN THE TREATMENT OF ARTHRITIS WITH TRADITIONAL CHINESE MEDICINE." In World Congress on Medical and Pharmaceutical Research (WCMPR 2017). Volkson Press, 2018. http://dx.doi.org/10.26480/wcmpr.01.2018.29.31.

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Palanisamy, V., and A. Kumarkombaiya. "Efficient analysis of pharmaceutical compound structure based on pattern matching algorithm in data mining techniques." In 2014 IEEE International Conference on Computational Intelligence and Computing Research (ICCIC). IEEE, 2014. http://dx.doi.org/10.1109/iccic.2014.7238456.

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